EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS031-14871 
Organism
Homo sapiens 
Tissue/cell
Denditric_cell 
Coordinate
chr22:50329920-50332920 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr22:50332208-50332223GGGTCACTGTGTCCT+6.14
MEF2BMA0660.1chr22:50330962-50330974GCTATTAATAGC+6.14
MEF2BMA0660.1chr22:50330962-50330974GCTATTAATAGC-6.14
MEF2BMA0660.1chr22:50330992-50331004GCTATAAATAGT+6.18
ZEB1MA0103.3chr22:50331448-50331459CCCACCTGCCC+6.14
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_03028chr22:50330257-50330910Bladder
SE_10057chr22:50329482-50331113CD14
SE_10530chr22:50329417-50331525CD19_Primary
SE_11301chr22:50322859-50332155CD20
SE_12420chr22:50329511-50330959CD3
SE_17545chr22:50326591-50331700CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50326643-50331570CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50329041-50330887Colon_Crypt_1
SE_23738chr22:50326901-50330921Colon_Crypt_2
SE_23738chr22:50330990-50331681Colon_Crypt_2
SE_24687chr22:50326851-50332818Colon_Crypt_3
SE_26808chr22:50326694-50332325Esophagus
SE_28169chr22:50329511-50330607Fetal_Intestine
SE_29459chr22:50329662-50330703Fetal_Intestine_Large
SE_31381chr22:50326539-50332985Gastric
SE_34375chr22:50329499-50331658HCT-116
SE_35007chr22:50329748-50331112HeLa
SE_42159chr22:50329569-50333037Lung
SE_47471chr22:50329736-50330581Pancreas
SE_47471chr22:50331041-50331735Pancreas
SE_49712chr22:50329828-50332142Right_Ventricle
SE_50117chr22:50329562-50332768Sigmoid_Colon
SE_52469chr22:50329581-50332615Small_Intestine
SE_53398chr22:50326561-50333542Spleen
SE_56937chr22:50327618-50330661VACO_400
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50329632-50332479Pancreatic_islets
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
SE_69071chr22:50329560-50330581H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr225033000050330846
chr225033072550331030
chr225033157150331948
chr225033224250332511
Enhancer Sequence
CCGGGGGCGG GGGCTCCCCG AAGGAAAGGA GCCCCCGCGG GAGCAGGCGC AGAATGAGAT 60
GCACGAGCGC CACCGCCGCC GCCGCACACC CCCCGCCCCC CCGGGGTGGA AGCCAGAACC 120
TGCGTCCCCA GCTCCCCCAG GCCCGCCCAC AGGGCGCCTG GCTGGGCCTC CGAGCTTTCC 180
TGTTTTCTCT GCAGCCTGGC TGGGCTTAGG GAGAGGTGGG GGGTGCGCCT CTTGATGCTG 240
GGGACGCGTG TGGCACAGGG AGCCGGGTGC AGCCAAGGCT TGGAGGGGTG CCCCCCGCCC 300
CACCCAGGTC ACACTTCACC CTTCGTGGGG TCGGGATCTG GTCTTTTTAC AAGCTAGGCG 360
CCCTCCCCCC TTTTTTTTTT TTTTTTTTTC TCAAAAATGA TCACAGGGAA TGAGCCTCAG 420
CCAGGACAGC GGGCTATGAG GCTGCCTGTT GCCCCCACCA GCCTGAATTC TGGCAGGGCC 480
CTTCTCCTCC ACCCACAGCC CTCCATCCAC ACCCCTCCAG TGGCTCCAAG GCCCATCTGA 540
CTTGGCCTCA GTTCACCTGT TTACTTCAGG GACACCTGGT TATACTGCCA GAGGCAGGTT 600
GGGGGGCCTG CAGGGCCGGC CTCTCTCAAA TCCACTTCTG GCTCTGCGGT CCCCACAGCA 660
CTTCCTTACC CCTTCCCCAT GCTGGAATCT GAGAACCAGA TATGGGGGTC CTGGTCTCAG 720
CATCCCTTTC CATCCGGGGT GCCCTGCTGC TGCCAGCTCA CGTGCCCACC ATCCCATCCT 780
CCTCAGGGTC AGTGTGGCTG CAGAACGGCC TCCGGGGAGA GCAGGGTGGG GGCTGTAGCC 840
TGGTGCACCC CCAGCCTGCT GTCCCAGGTG AATGCAGACC CCTGGCTCAG CTGCTGACCA 900
GATAACAGTG GCCCTTGTGC CGAAGCCTGG GTGGGGGCTG GGGTACCAGC CCCGGGTGTC 960
TCCGGGCACA GAATGGCACC CACCCCCACC CCACCCGCAG GCAGCGGCCA GCAGGAGACA 1020
TTGTCCGTCC CCCTCAACCC TGGCTATTAA TAGCTCCTCT GGGCTAGGAG CGGCTATAAA 1080
TAGTCCCAGC CCCTCACACA GGCCCATTCA GGCACCCGCT GCCTGGGTGT GCACAGCAGC 1140
CACACTTGCG CTCACTCAGA GCTGTGCACG CGGGAACCGT GCCACTTCTG CCCCTCCACG 1200
CCATCTGCAC TGCACAGATC CAGGCTGTCC CTGCAGCCCT CACTGGGTCT CCTGTGGCAG 1260
GGGAGGGCCC TGAACCCTCT GGAGGCTTTT CCCTTGCCCC CTCCCGCCAC GCCCAGGGTC 1320
CCCTTGGGGC TTCTAGCTAC TCTAGGGTCT TGCTCTGGGG CTTCTGGAAG TCAGATGCAT 1380
TCACCCAAAG CCAGCCTGGG GCGGGGGGAG GTCCACCTGG AGGGAGGCCC AGCCCCTGCA 1440
GAGACCTAAG CCTGGCCTCT GCCCCAAGCA CTGCTGCCTC GGGCCATGAG GCTCACAGGG 1500
TCTCCTTAGC CCAAGGCTGG TCCAGCCTCC CACCTGCCCT GTGGGGCAGA CGTCACTGAA 1560
TTCCCACTCC TTGCCCTGGA GGCCTCATTG CCGTCAACTA GGCTATGGCC CCCACTGTGA 1620
CTCCCACTCC CAGGGTGACA GAATGGGCAC CTGGTCCAGG AAAGCCTGCT CTGTGGACCC 1680
CCTACCCGTC CACACTGTCC ACGCCCCATG GCTAGTGGTG ACAGGAGACA GGATGGGGGG 1740
CATGGGGGCT GCTGTTATTG TGTCCAGAGG AGAAAAGGAA AACAATCCTG TTTACGGAAA 1800
AGGAATGTCC GTCCACTGCC GCCAGCCAGT GGCCTTCCTG GGGGGACAGA GGCCCTTTGT 1860
TGGGAAAACA GGAAGCGAGG ATTTCCAGGA TCTGCCAGGC CGCCCGCCGG CCACCCGCCC 1920
CACTTCCGCC AATTCTCGGC AGCCTGCGCT GGCCACCAGC TGCCCGTCGG TCCATCCACG 1980
TTTCTGTCTA TCCGTCTGAC CGTGGGGCCC AGGCGTACAG CCTTAGCACA TCCTGCTCTA 2040
TGTGGTGCCT CAGTCACACA GGGACAAACA CCCACAGGGT CCTCGCAGGG CCTGGGAGGG 2100
CTGCCTGGGA GCTGAGACCC AAGGAGTGAG GACCCGTGCC CCACATAGGG AAGGGCAGTG 2160
CCAGACATGG AGAAGGCGGA TGGGGCAGGG GCCACGGGCC AGGAACCGGG GAGGCGGGAA 2220
CAGCCAAAGG GAAGCTGTGC CAGACTCTCC CCTCCCCACC CAAGAGCCAG GGATGGTTTT 2280
GGGGTTAGGG GTCACTGTGT CCTTACTACC CAAACCCACT TACAGTCCAT GGCCCACGCG 2340
ATGCTCGCCT GTCACTGACC CGGGACAGCA TGGGCTCACT CGTGCATGAA CACCAGACGT 2400
GTGTACACTC AGCGGACACT CACCTGTGCA CACACAGCAC ACACGTGCAC ACACCACGGA 2460
CACTCTGACC TGTGCACACA CAGCACACAC GTGCACACTC AGCGGACACT CACCTGTGCA 2520
CACACAGCAC ACACGTGCAC ACACCAGCAC CCCCCAGCAC GGATGCAGGC ACCGTCATGA 2580
GCACGGAGAC CACCCCAGGA CACCAGCAGC TGCACCCCCC GGCGGGGCTG CACTGGCCGA 2640
CAGTGCCCAG GGGACTGCTC CCAGCCCCTG TGGGGGGCTT CTGTGATTCT GTGTGGGTTC 2700
CTGTGTGCCC TGTTTGGGCT CTCACCGGTC AGAGGGGGCT GGCACAGTGC CTGTGACCTC 2760
AGTCCTGGGC AGGGCCAGGA GGTGCCAGGA GCAGGCAGGC CTGGGGCAGG ACTCTGTTTA 2820
GGGCCAGCTG GAGGACCCTC TGCCCCCACC TCCACATCCC AAGTCGGCAG CTTCCTCCCA 2880
CTGTGGTGGT GATACAGGAG ATAGAAAGAA ATTATTTAGG TAGATAATGA GGGCAAAAGA 2940
GTCCTCAGCA GAACCTCCCT TCTAACAAAA AGCAGGCCCG GGCGAGGTGG CTCACAGCTG 3000